Toner resin composition and toner
AssigneeSekisui Chemical Co., Ltd.
InventorsHiroaki Takehara, Takashi Ueyama, Masazumi Okudo
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AssigneeSekisui Chemical Co., Ltd.
InventorsHiroaki Takehara, Takashi Ueyama, Masazumi Okudo
Estimating the term…
A toner resin composition composed of a vinyl-type copolymer which has styrene-type monomers and (meth)acrylic ester-type monomers as the main ingredients, a low-melting-point crystalline compound, and a block compolymer of polystyrene and polyolefin wherein the average particle area is 0.5-20 μm2 and the maximum particle area is 30 μm2 or less in any 25 μm×25 μm area when transmission electron microscopy is used to observe said low-melting-point crystalline compound which forms domains in the domain-matrix structure formed by said vinyl-type copolymer and the low-melting-point crystalline compound. To provide a toner resin composition and toner which have superior fixability, anti-offset properties, and shelf stability.
A toner resin composition comprising:
A toner comprising:
Dependencies are inferred from the claim text.
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Plasticisers; Charge controlling agents: organic compounds
With toner particles: characterised by the dimensions of the particles
With toner particles: characterised by their structure; characterised by non-homogenuous distribution of components
Copolymers of styrene: with esters of acrylic or methacrylic acid
Term ended 5 Oct 2019 (estimated)
USPTO file history isn’t available for this patent, so only indexed dates are shown.
1. Field of the Invention
The present invention relates in general to a toner resin composition and toner used in electrophotography and such, and more particularly to a toner resin composition and toner used in the so-called dry developing method for developing electrostatic charge images.
2. The Prior Art
Examples and Comparative examples of the present invention are shown below.
30 weight parts of a vinyl-type copolymer with a peak molecular weight value of 500,000 obtained by polymerizing a mixture composed of 80 wt % styrene and 20 wt % N-butyl acrylate, 4 weight parts of the low-melting-point crystalline compound (A) shown in Table 1, 1 weight part of the block copolymer of polystyrene and polyolefin (a) shown in Table 2, and 100 weight parts of toluene were put into a flask and dissolved. After purging the inside of the flask with nitrogen gas, the temperature was raised to the boiling point of toluene. As toluene was refluxing and the mixture was being stirred, a mixture of 50 weight parts of styrene, 15 weight parts of N-butyl acrylate and 3.8 weight parts of benzoyl peroxide (polymerization starter) was dripped into it over a period of three hours to carry out the coexistent solution polymerization. After completion of the dripping, stirring continued with toluene refluxing for one more hour for maturation, and a low molecular weight polymer with a molecular weight peak value of 8,000 was polymerized.
The temperature in the flask was then gradually raised up to 180° C. at a reduced pressure to remove toluene and obtain a resin. After cooling, this resin was crushed to obtain the toner resin composition of the present invention.